Trisomy 8q - CISMeF

Preferred Label : Trisomy 8q;

NCIt definition : A chromosomal rearrangement characterized by the presence of a third copy of the long arm of chromosome 8 (8q) in a cell.;

Details

Origin ID

C36428;

UMLS CUI

C0795829;

Currated CISMeF NLP mapping
- 8q duplication [ICD-11 More detail]
- Chromosome 8, trisomy 8q [MeSH concept]
- Trisomy 8q syndrome [ORDO Disease]
- chromosome 8, trisomy 8q [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 8q duplication [ICD-11 More detail]
- Chromosome 8, trisomy 8q [MeSH concept]
- Trisomy 8q syndrome [ORDO Disease]
- chromosome 8, trisomy 8q [MeSH Supplementary Concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 8 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Recurrent T-Cell Prolymphocytic Leukemia [NCIt concept]
- Refractory T-Cell Prolymphocytic Leukemia [NCIt concept]
- Splenic Manifestation of T-Cell Prolymphocytic Leukemia [NCIt concept]
- T-Cell Prolymphocytic Leukemia [NCIt concept]
- T-Cell Prolymphocytic Leukemia Involving the Skin [NCIt concept]
- T-Cell Prolymphocytic Leukemia, Cerebriform Cell Variant [NCIt concept]
- T-Cell Prolymphocytic Leukemia, Small Cell Variant [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients